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Ann Thorac Surg 2008;85:1536. doi:10.1016/j.athoracsur.2008.02.044
© 2008 The Society of Thoracic Surgeons

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Original Articles: Adult Cardiac

Invited Commentary

Robert A.E. Dion, MD, PhD

Department of Cardiac Surgery, Ziekenhuis Oost-Limburg – Campus St. Jan, Schiepse Bos 6, Genk 3600, Belgium

(Email: robert.dion@zol.be).

The first 20% of the full text of this article appears below.

The authors [1] conclude that intrinsic mitral valve (MV) pathology is frequently observed in hypertrophic cardiomyopathy (HCM) and that durable repair is feasible in only approximately half of the patients. I would add that this is only done by experienced surgeons, indeed, as a prosthetic valve has no systolic anterior motion (SAM) of the mitral coaptation line, and the authors have not been able to demonstrate a difference in survival between repair and replacement.

Their analysis identified 6 nonmutually exclusive groups, but why is a "long-leaflets group" different from the degenerative and myxomatous ones? Also, I hardly distinguished . . . [Full Text of this Article]


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Mitral Valve Abnormalities in Hypertrophic Cardiomyopathy: Echocardiographic Features and Surgical Outcomes
Ryan K. Kaple, Ross T. Murphy, Linda M. DiPaola, Penny L. Houghtaling, Harry M. Lever, Bruce W. Lytle, Eugene H. Blackstone, and Nicholas G. Smedira
Ann. Thorac. Surg. 2008 85: 1527-1535. [Abstract] [Full Text] [PDF]






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